How ubiquitination regulates the TGF-β signalling pathway: New insights and new players New isoforms of ubiquitin-activating enzymes in the E1-E3 families join the game

被引:25
作者
Soond, Surinder M. [1 ]
Chantry, Andrew [1 ]
机构
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
关键词
cancer; EMT; Smad; TGF-beta; ubiquitination; ubiquitinome; PROTEASOME-DEPENDENT DEGRADATION; SMAD4 PROTEIN STABILITY; CYCLE MUTANT TS85; HECT DOMAIN; PROMOTES DEGRADATION; NEGATIVE REGULATION; LIGASE ACTIVITY; STEM-CELLS; I RECEPTOR; C2; DOMAIN;
D O I
10.1002/bies.201100057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitination of protein species in regulating signal transduction pathways is universally accepted as of fundamental importance for normal development, and defects in this process have been implicated in the progression of many human diseases. One pathway that has received much attention in this context is transforming growth factor-beta (TGF-beta) signalling, particularly during the regulation of epithelial- mesenchymal transition (EMT) and tumour progression. While E3-ubiquitin ligases offer themselves as potential therapeutic targets, much remains to be unveiled regarding mechanisms that culminate in their regulation. With this in mind, the focus of this review highlights the regulation of the ubiquitination pathway and the significance of a recently described group of NEDD4 E3-ubiquitin ligase isoforms in the context of TGF-beta pathway regulation. Moreover, we now broaden these observations to incorporate a growing number of protein isoforms within the ubiquitin ligase superfamily as a whole, and discuss their relevance in defining a new 'iso-ubiquitinome'.
引用
收藏
页码:749 / 758
页数:10
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